Progeria.
Article
in En
| IMSEAR
| ID: sea-139786
ABSTRACT
Hutchinson Gilford Progeria Syndrome (HGPS) is a rare, sporadic, autosomal dominant syndrome that involves premature ageing and death at early age due to myocardial infarction or stroke. A 30-year-old male with clinical and radiologic features highly suggestive of HGPS is presented here with description of differential diagnosis, dental considerations and review of literature.
Key words
Full text:
1
Index:
IMSEAR
Main subject:
Parietal Bone
/
Progeria
/
Humans
/
Male
/
Nose
/
Craniofacial Abnormalities
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Adult
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Cranial Sutures
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Diagnosis, Differential
/
Frontal Bone
Type of study:
Diagnostic_studies
Language:
En
Year:
2009
Type:
Article